Key result
Substituting the viral CMV promoter with synthetic promoters in CHO cells reduced aberrant protein contaminants and improved expression of a difficult-to-express mAb.
Synthetic promoters provide tunable transcriptional activity in CHO cells, improving the yield and quality of complex recombinant proteins compared to traditional viral promoters.
Synthetic promoters enable tunable rProtein expression; leaves open scalability and yield gains in manufacturing.
When expressing complex biotherapeutic proteins, traditional expression plasmids and methods may not always yield sufficient levels of high-quality product. High-strength viral promoters commonly used for recombinant protein (rProtein) production in mammalian cells allow for maximal expression, but provide limited scope to alter their transcription dynamics. However, synthetic promoters designed to provide tunable transcriptional activity offer a plasmid engineering approach to more precisely regulate product quality, yield or to reduce product related contaminants. We substituted the viral promoter CMV with synthetic promoters that offer different transcriptional activities to express our gene of interest in Chinese hamster ovary (CHO) cells. Stable pools were established and the benefits of regulating transgene transcription on the quality of biotherapeutics were examined in stable pool fed-batch overgrow experiments. Specific control of gene expression of the heavy chain (HC):light chain (LC) of a Fab, and the ratio between the two HCs in a Duet mAb reduced levels of aberrant protein contaminants; and the controlled expression of the helper gene XBP-1s improved expression of a difficult-to-express mAb. This synthetic promoter technology benefits applications that require custom activity. Our work highlights the advantages of employing synthetic promoters for production of more complex rProteins.
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Sou et al. (2023) studied this question. Synthetic promoters vs. Viral promoter CMV was evaluated on Expression and product quality of biotherapeutic proteins. Substituting the viral CMV promoter with synthetic promoters in CHO cells reduced aberrant protein contaminants and improved expression of a difficult-to-express mAb.
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